SUTURES POLYPROP., POLYETHELINE, NYLON & SILK
K-Number: K930739 · 1994-07-26
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Device Summary
Frequently Asked Questions
What is the SUTURES POLYPROP., POLYETHELINE, NYLON & SILK?
SUTURES POLYPROP., POLYETHELINE, NYLON & SILK is a medical device that received FDA 510(k) clearance on 1994-07-26. The listed applicant is Deknatel, Inc.. The 510(k) number is K930739.
When did SUTURES POLYPROP., POLYETHELINE, NYLON & SILK receive FDA 510(k) clearance?
SUTURES POLYPROP., POLYETHELINE, NYLON & SILK received FDA 510(k) clearance on 1994-07-26, under 510(k) number K930739.
Who is the listed applicant for SUTURES POLYPROP., POLYETHELINE, NYLON & SILK?
The FDA 510(k) record lists Deknatel, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUTURES POLYPROP., POLYETHELINE, NYLON & SILK?
The FDA product code for SUTURES POLYPROP., POLYETHELINE, NYLON & SILK is GAP.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Deknatel, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: GAP)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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